NDC 69267-101 Atenolol Scopolamine

Product Information

Product Packages

NDC 69267-101-06

Package Description: 151.5 mg in 1 BOTTLE, PLASTIC

NDC 69267-101-12

Package Description: 303 mg in 1 BOTTLE, PLASTIC

NDC 69267-101-24

Package Description: 606 mg in 1 BOTTLE, PLASTIC

NDC 69267-101-48

Package Description: 1212 mg in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Atenolol Scopolamine is product labeled by Tps. The product's dosage form is and is administered via form.


What are Atenolol Scopolamine Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • ATENOLOL (UNII: 50VV3VW0TI)
  • ATENOLOL (UNII: 50VV3VW0TI) (Active Moiety)
  • SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB)
  • SCOPOLAMINE (UNII: DL48G20X8X) (Active Moiety)


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Atenolol Scopolamine Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

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